About The Position

In accordance with established policies, procedures, and study protocols, this position provides support for clinical research studies. Responsibilities include recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy and EKGs; and maintaining and updating data generated by the study. Additionally, the role involves assessing study subject suitability and contributing to recruitment strategies. Tasks also include data analysis, interpretation, quality assurance and control (QA/QC), and assisting in the completion of reports and presentations.

Requirements

  • Bachelor's Degree Science required
  • Related post-bachelor's degree research experience 1-2 years required
  • Ability to work more independently and as a team member.
  • Computer literacy, analytical skills, and ability to resolve technical problems.
  • Ability to interpret the acceptability of data results.
  • Working knowledge of data management programs.

Nice To Haves

  • Can this role accept experience in lieu of a degree? Yes

Responsibilities

  • Assists in determining the suitability of study subjects and acts as a resource for patients and their families.
  • Contributes to recruitment strategies and may provide input on protocol recommendations.
  • Administers assessments and evaluates study questionnaires.
  • Maintains research data, patient files, regulatory binders, and study databases.
  • Performs data analysis and QA/QC checks, organizing and interpreting data as needed.
  • Aids in preparation for annual reviews and assists the Principal Investigator in completing study reports and presentations.
  • May assist in training and orientation for new staff members.

Benefits

  • comprehensive benefits
  • career advancement opportunities
  • differentials
  • premiums
  • bonuses as applicable
  • recognition programs
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